CN112480616B - Melamine salt reinforced low-temperature thermoplastic material and preparation method thereof - Google Patents

Melamine salt reinforced low-temperature thermoplastic material and preparation method thereof Download PDF

Info

Publication number
CN112480616B
CN112480616B CN202011284739.1A CN202011284739A CN112480616B CN 112480616 B CN112480616 B CN 112480616B CN 202011284739 A CN202011284739 A CN 202011284739A CN 112480616 B CN112480616 B CN 112480616B
Authority
CN
China
Prior art keywords
polycaprolactone
melamine
temperature thermoplastic
thermoplastic material
melamine salt
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN202011284739.1A
Other languages
Chinese (zh)
Other versions
CN112480616A (en
Inventor
吴嘉梁
章中群
邱锡波
刘海宏
林才生
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Klarity Medical & Equipment Gz Co ltd
Original Assignee
Klarity Medical & Equipment Gz Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Klarity Medical & Equipment Gz Co ltd filed Critical Klarity Medical & Equipment Gz Co ltd
Priority to CN202011284739.1A priority Critical patent/CN112480616B/en
Publication of CN112480616A publication Critical patent/CN112480616A/en
Application granted granted Critical
Publication of CN112480616B publication Critical patent/CN112480616B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/24Crosslinking, e.g. vulcanising, of macromolecules
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/10X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/28Treatment by wave energy or particle radiation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/10X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
    • A61N2005/1092Details
    • A61N2005/1097Means for immobilizing the patient
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2367/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2367/04Polyesters derived from hydroxy carboxylic acids, e.g. lactones
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477Six-membered rings
    • C08K5/3492Triazines
    • C08K5/34924Triazines containing cyanurate groups; Tautomers thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477Six-membered rings
    • C08K5/3492Triazines
    • C08K5/34928Salts

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Pathology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Radiology & Medical Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

A melamine salt reinforced polycaprolactone low-temperature thermoplastic material and a preparation method thereof. Compared with the existing polycaprolactone type low-temperature thermoplastic product, the formed low-temperature thermoplastic material has lower contractility and better fixing effect in use, so that the low-temperature thermoplastic material is more suitable for hospitals or other radiotherapy units and is matched with three-dimensional conformal radiotherapy instruments for use in tumor operations or rehabilitation orthopedic equipment.

Description

Melamine salt reinforced low-temperature thermoplastic material and preparation method thereof
Technical Field
The invention relates to a low-temperature thermoplastic material, in particular to a fixing material for low-temperature thermoplastic radiotherapy and rehabilitation orthopedic treatment and a preparation process thereof.
Background
The low-temperature thermoplastic material is prepared by taking polycaprolactone as a main component and adding additives, and is characterized in that: it can be softened and molded into any shape when heated to a certain temperature (about 65 ℃), and has the rigidity of plastic when cooled to normal temperature. The characteristics can be used for accurate positioning of tumor patients during radiotherapy or fixation of fracture parts during rehabilitation and orthopaedics. The low-temperature thermoplastic material is widely used for preparing radiotherapy positioning membrane products and in the field of rehabilitation orthopedics at present.
Although the existing polycaprolactone type low-temperature thermoplastic radiotherapy positioning product is convenient to form, the shrinkage force is large in the forming process, and strong compression force can be generated on a patient, so that severe discomfort can be caused. Moreover, because the rigidity of the raw materials is insufficient, the deformation resistance after shaping is poor, and the shaking of the key parts of the patient in the treatment process can seriously affect the precision and the radiotherapy quality of the later-stage tumor radiotherapy.
In order to solve the problem of how to improve the comfort of patients and the precision of radiotherapy in the radiotherapy process, at present, a polycaprolactone + carbon fiber composition (Chinese patent, grant publication No. CN101062977B) which can reduce the contractility and has better fixing strength is provided, but the carbon fiber can influence the imaging effect of nuclear magnetic resonance equipment, and because the resolution of nuclear magnetic resonance on soft tissues is superior to that of other equipment, nuclear magnetic resonance imaging technology is adopted in more and more radiotherapy departments, so the carbon fiber low-temperature thermoplastic material is limited in clinical application.
Foreign countries also have reinforced low temperature thermoplastic materials made of kevlar + polycaprolactone, which, although well fixed, is very expensive.
In order to overcome the above problems, the inventors have also attempted to overcome the above problems by compounding polycaprolactone with glass fiber. The imaging effect of the nuclear magnetic resonance equipment cannot be influenced by the glass fibers, and the pulling force and the pressing force of the material can be obviously reduced while the strength is improved by the glass fibers in a certain proportion.
Melamine and condensation products and salts thereof are widely used as flame retardants, with melamine salts being a class of nitrogen-based or nitrogen-phosphorus-based flame retardants, such as melamine cyanurate and the like, being common. Generally, such melamine salts are added to the matrix as flame retardants, along with other reinforcing components.
Disclosure of Invention
The novel low-temperature thermoplastic material for positioning in radiotherapy is prepared by combining the special requirements of the low-temperature thermoplastic material for radiotherapy, has higher rigidity and fixing effect than common low-temperature thermoplastic materials, and has the advantages of lower shrinkage force, easiness in stretching and shaping, lower cost and the like.
In order to achieve the above object, a first aspect of the present invention provides a melamine salt reinforced low temperature thermoplastic material, which is composed of polycaprolactone and melamine salt, and has a gel content of 20% or more (i.e., the material has a certain crosslinked network structure, and the gel content measured in a good solvent is 20% or more); wherein the melamine salt is melamine cyanurate, melamine polyphosphate or melamine phosphate, and the mass ratio of the polycaprolactone to the melamine salt is 90:10-60:40 (namely, the melamine salt accounts for 10% -40% of the total mass of the polycaprolactone and the melamine salt).
Among them, melamine cyanurate, CAS No.: 37640-57-6. Melamine polyphosphate, CAS No.: 218768-84-4. Melamine phosphate, CAS No.: 20208-95-1.
The gel content refers to gel content data obtained by measuring the whole product. Specifically, the product with 20% to 100% gel content is obtained by the parameter control of the crosslinking process (kind and amount of crosslinking agent; crosslinking process parameters such as irradiation dose and time) according to the needs of product cost and efficiency. In some embodiments, the gel content may be 20%, 30%, 40%, 50%, 70%, or 100%.
The method for measuring the gel content comprises the following steps: weighing a sample with the mass m1, adding the sample into a solvent, placing the sample in a proper environment, extracting the sample after swelling, drying the sample until the mass is constant, and weighing the mass m 2. The gel content is Vc m2/m1 x 100%.
In some embodiments, the specific method of determining the gel content is: weighing a sample with the mass m1, putting the sample into a ground bottle filled with 25mL of toluene, tightly covering the bottle cap, putting the bottle in a constant-temperature oven at 25 ℃ to swell for 48 hours, and taking out the sample. The sample was then extracted for 24 hours and finally the sample was dried in a vacuum oven at 50 ℃ until the mass was constant and the mass was weighed to give a mass m 2. The gel content is Vc m2/m1 × 100%.
Specifically, in some embodiments, the mesh size of the melamine salt is 800-.
The low-temperature thermoplastic material is a composite material taking polycaprolactone as a matrix, and the required low-temperature thermoplastic material can be obtained by generally subjecting raw materials (polycaprolactone and melamine salt) to forming and crosslinking processes. Thus, a second aspect of the present invention is to provide a process for the production of the above low temperature thermoplastic material obtained by subjecting polycaprolactone and melamine salt to a forming and crosslinking process.
Specifically, the method for manufacturing the low-temperature thermoplastic material comprises the following steps:
(1) mixing polycaprolactone, melamine salt and a cross-linking agent to obtain a composition; wherein the mass ratio of polycaprolactone to melamine salt is 90:10-60: 40;
(2) carrying out a molding process on the uniformly mixed composition to obtain a blank;
(3) and (3) carrying out a cross-linking process on the blank to obtain the low-temperature thermoplastic material with the gel content of more than or equal to 20%.
Specifically, the molding process in the above method refers to a process of forming plastic raw materials in various forms (powder, granule, solution and dispersion) into a product or blank in a desired shape by a specific method. Generally, the process comprises heating the raw materials to a fluid state (e.g., molten state), then obtaining a shape by, for example, placing in a mold, and finally cooling and setting.
Specifically, in some embodiments, the polycaprolactone of step (1) has a weight average molecular weight of 40000-.
Specifically, in some embodiments, the melamine salt is employed in a mesh size of 800-10000 mesh.
It will be understood that the present invention is not intended to be limited to the shape of the blank and the final product. In some embodiments, the blank and ultimately the cryogenic thermoplastic material is a sheet material in order to produce a radiation therapy positioning product suitable for a specific location. In other embodiments, the material can be a film, a tube, a plate, a bar, a strip, or other special-shaped material with a complex cross section; for example, in other embodiments where the product is used for finger positioning, the blank and ultimately the low temperature thermoplastic material may be tubing.
To obtain blanks of different shapes, the present invention may employ various suitable forming methods including, but not limited to, injection, extrusion, calendering, blow molding, and the like. For example, in some embodiments, to obtain a sheet for a radiotherapeutic positioning product, the above composition may be heated to a molten state (generally, a heating temperature of 65 ℃ to 160 ℃), and then sheet-shaped by, for example, an extrusion or injection process. In addition, as a process well known to those skilled in the art, in order to obtain effects such as ventilation and heat dissipation during use (radiotherapy), the sheet (blank) may be perforated (punched) as required before or after crosslinking. For example, a punching machine can be used to punch holes in a specific mesh ratio before the crosslinking process; this proportion may be between 1% and 50% according to the specific application and requirements.
It is to be noted that the present invention is characterized by limiting the filler to a specific melamine salt, and to a specific amount and/or mesh thereof, rather than to the material forming process. The invention has universality to the common molding process; compared with the prior art, the invention can obtain the beneficial effects stated in the specification under the condition of adopting the same process indexes.
Specifically, the crosslinking process in the above method refers to a process of forming a network or a body-type polymer by covalent bonds among the chains of the polymer (polycaprolactone) in the raw material, and includes chemical crosslinking and physical crosslinking. Physical crosslinking is the crosslinking of polymers by irradiation with light, heat, or the like. For the purposes of the present invention, the usual crosslinking methods for polycaprolactone can be employed. In some embodiments, the present invention employs irradiation crosslinking, the irradiation source may be a high energy electron accelerator, a cobalt source, X-rays or ultraviolet light, and the irradiation dose is 2-30KGy, preferably 2-10KGy, more specifically 4-7 KGy; for example, in some embodiments the dose is 4KGy, and in other embodiments the dose is 7 KGy.
The cross-linking agent allows the polycaprolactone to cross-link under the appropriate conditions and to obtain a low-temperature thermoplastic material. Commonly used cross-linking agents include triallyl isocyanurate, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, pentaerythritol triacrylate, ethylene dimethacrylate. Generally, the amount of conventional cross-linking agent is 0.05% to 5% of the total mass of polycaprolactone and melamine salt, depending on the requirements of the target product. In some embodiments, the crosslinker is triallyl isocyanurate.
It is to be noted here that the present invention is characterized by limiting the filler to the melamine salt and to its specific amount and/or mesh number, rather than by the process of crosslinking the material. The invention has universality to the common crosslinking process suitable for polycaprolactone; compared with the prior art, the invention can obtain the beneficial effects stated in the specification by adopting the same process index as long as the cross-linking process can obtain the target gel content.
According to the requirements of product cost and efficiency, the product with 20 percent to 100 percent of gel content is obtained through the parameter control of the crosslinking process (the type and the dosage of the crosslinking agent; the parameters of the crosslinking process such as irradiation dose and time). In some embodiments, the gel content may be 20%, 30%, 40%, 50%, 70%, or 100%. For example, in some embodiments, the crosslinking agent triallyl isocyanurate is used for radiation crosslinking at a suitable dose, and the radiation dose is selected to be 7KGy, and the required gel content can be obtained by controlling the radiation time. For example, in some embodiments, the gel content obtained is 40%; while in other embodiments, the gel content obtained is 20%, 30%, 50%, 70%, or 100%.
It will be understood that the process for the preparation of the low-temperature thermoplastic material according to the invention is not limited solely to the above-listed processes. The polycaprolactone-based composite material with corresponding component content and gel content can also be obtained by other methods in the prior art.
The low-temperature thermoplastic material can be applied to the fixation/positioning of human body parts or joints, particularly when a nuclear magnetic resonance imaging technology is adopted; because the imaging effect of nuclear magnetic resonance equipment can be influenced by common materials such as carbon fiber and the like, the polycaprolactone/melamine salt composite low-temperature thermoplastic material is more suitable for a positioning technology adopting a nuclear magnetic resonance imaging technology.
A third aspect of the present invention therefore consists in providing the use of the above-mentioned cryogenic thermoplastic material for the preparation of a device for immobilizing a body part or joint, in particular for preparing a device suitable for use in magnetic resonance imaging techniques. The device for immobilising a body part or joint is obtained by making a low temperature thermoplastic material into a specific shape suitable for storage, transport or application. The specific shape suitable for storage, transportation or application may be obtained by customizing a mold in a molding process, or by a method such as cutting before a crosslinking process after the molding process, or by a method such as cutting after the crosslinking process.
In particular, in some embodiments, the material can be used to prepare fixation devices for radiation therapy, such as head and neck and shoulder positioning films, body positioning plates, and the like. Of course, the cryogenic thermoplastic material is not limited to the preparation of positioning devices for radiation therapy. In view of its low temperature thermoplastic properties, and suitable stiffness and shrinkage force parameters, it is also applicable to other aspects including, but not limited to: fixation after surgical treatment of soft tissue injury such as joint ligament and nerve tendon injury; fixation after fracture and joint dislocation reduction; fixation after burns and other orthopedic surgery. For example, the method can be used for preparing fracture fixation splints. Since these aspects may also relate to the use of magnetic resonance imaging techniques, the use of the present invention would be advantageous and less restrictive than other prior art polycaprolactone low temperature thermoplastic materials.
In a fourth aspect of the invention, a device for immobilising a body part or joint is provided, the body of which is made of a low temperature thermoplastic material as described above. It will be readily appreciated that, in addition to the body made of the aforementioned low-temperature thermoplastic material, the device may also comprise other auxiliary parts, such as straps, etc. for auxiliary fixing.
The use method of the device mainly comprises the following steps:
(1) placing the device in an environment at the softening temperature of the low-temperature thermoplastic material so that the device softens;
(2) placing the softened device on a part or joint to be fixed for shaping;
(3) and cooling and shaping the device.
Specifically, the above softening temperature is 60 to 70 ℃ depending on the composition of the material. Thus, step (1) may be carried out by placing the device in water at 60-70 ℃ so that the device softens.
Specifically, the cooling setting of the material (device) is generally performed below the softening temperature. In order to make the human body comfortable, step (3) is preferably performed at normal or room temperature. In some embodiments, step (3) is performed at 15 ℃ to 30 ℃.
The comprehensive performance of the low-temperature thermoplastic material can meet the application requirement and is superior to other materials, particularly the bending strength; under the same addition amount (5% -35%), the melamine salt material is superior to other reinforced filling materials suitable for the nuclear magnetic resonance imaging technology, and the deformation resistance is stronger. When being applied to human body part fixedly, for example radiotherapy location, because radiotherapy location diaphragm effect is fixed patient's head or parts such as neck chest, prevent that radiotherapy in-process patient from removing, the resistant deformability of diaphragm material is better, then the fixity after moulding on patient's health is better. That is, the fixing accuracy of the diaphragm made of the low-temperature thermoplastic material of the present invention is higher than that of the diaphragm made of other reinforced filling materials, especially other reinforced filling materials suitable for the magnetic resonance imaging technology.
In addition to flexural strength, the low temperature thermoplastic material of the present invention also has a lower cold set stress than other materials. In the application of human body part/joint fixation, the material is used for preparing a fixing device, the part/joint fixation is realized through the process of firstly heating for softening and then cooling and shaping at normal temperature, and the lower the cooling compression force is, the higher the comfort of a user in clinic is.
Finally, the beneficial effects of the invention are as follows: experiments prove that compared with the existing polycaprolactone type low-temperature thermoplastic product, the low-temperature thermoplastic material prepared by the invention has smaller contractility after forming, better comfort and better fixing strength, thereby being more suitable for hospitals or other radiotherapy units and being matched with a three-dimensional conformal radiotherapy instrument for fixing fracture parts in tumor operations or rehabilitation and orthopedics.
In general, melamine-based flame retardants (such as melamine cyanurate) only act as flame retardants in composite materials, and as a single component do not generally significantly improve the mechanical properties of the material. The inventor finds that the flame retardant is compounded with polycaprolactone, so that the flame retardant capability of the material is endowed, and the mechanical property of the material can be obviously improved. The polycaprolactone and the melamine salt flame retardant are compounded according to a specific proportion, so that the strength of the material can be obviously improved, and furthermore, two parameters of the shaping pulling force and the cooling deformation pressing force of the material are obviously optimized. Especially, when the mesh number of melamine salt is 2000-10000 and the content is 25% -35%, the pulling force and/or the pressing force of the material is further reduced. The low temperature thermoplastic material and the fastening device of the present invention will thus be more suitable for applications involving stretching, especially stretching to a certain extent or more. This optimized phenomenon is exhibited in the range of 20% to 100% of gel content, particularly in the range of 20% to 70%, and more particularly in the range of 20% to 50%.
Detailed Description
The materials and effects of the present invention are described in detail below by way of exemplary embodiments. It is noted that certain parameters in the following exemplary embodiments will employ uniform values (such as the type and amount of cross-linking agent) in order to facilitate lateral comparison of the effect data, but this is not intended to represent that the benefits claimed in this specification cannot be obtained when other types or values recited in the specification are employed. The claimed advantageous effects can be achieved by using a certain value or kind within the range described in the specification, and the description is not repeated herein for reasons of space limitation.
Example 1
Preparation of materials
1. Method for preparing material
The material was prepared according to the following steps:
(1) the base material, the filler and the crosslinking agent are stirred to obtain a uniform mixture.
(2) In a double-screw granulator, the mixture is melted, blended and extruded into granules, and the melting temperature is between 60 and 150 ℃.
(3) And (3) carrying out calendering molding on the cut pellets in extrusion calendering equipment, wherein the processing temperature is between 60 and 150 ℃.
(4) Irradiating the sheet material by a linear accelerator with gamma ray at an irradiation dose of 7KGy, and controlling the irradiation time to obtain the low-temperature thermoplastic material with the required gel content.
2. Gel content determination method
The gel content of the product was determined by the following steps:
weighing a sample with the mass m1, putting the sample into a ground bottle filled with 25mL of toluene, tightly covering the bottle cap, putting the bottle in a constant-temperature oven at 25 ℃ to swell for 48 hours, and taking out the sample. The sample was then extracted for 24 hours and finally the sample was dried in a vacuum oven at 50 ℃ until the mass was constant and the mass was weighed to give a mass m 2. The gel content is Vc m2/m1 × 100%.
Material 1:
substrate polycaprolactone (weight average molecular weight 50000). The filler melamine cyanurate (mesh number 800) and the proportion of filler (i.e. the proportion of filler in the total mass of substrate and filler) was 15%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 2:
base material polycaprolactone (weight average molecular weight 50000). The filler is melamine cyanurate (mesh number 800), and the proportion of the filler is 25%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 3:
base material polycaprolactone (weight average molecular weight 50000). The filler is melamine cyanurate (mesh number 800), and the proportion of the filler is 35%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 4:
base material polycaprolactone (weight average molecular weight 50000). The filler melamine cyanurate (mesh number 2000) and the proportion of filler were 15%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 5:
base material polycaprolactone (weight average molecular weight 50000). The filler melamine cyanurate (mesh number 2000) and the proportion of filler were 25%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 6:
substrate polycaprolactone (weight average molecular weight 50000). The filler melamine cyanurate (mesh number 2000) and the proportion of filler were 35%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 7:
substrate polycaprolactone (weight average molecular weight 50000). The filler is melamine cyanurate (mesh number 5000), and the proportion of the filler is 15%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 8:
base material polycaprolactone (weight average molecular weight 50000). The filler is melamine cyanurate (mesh number 5000), and the proportion of the filler is 25%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 9:
substrate polycaprolactone (weight average molecular weight 50000). The filler is melamine cyanurate (mesh number 5000), and the proportion of the filler is 35%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 10:
base material polycaprolactone (weight average molecular weight 50000). The filler is melamine cyanurate (mesh number 10000), and the filler proportion is 15%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 11:
base material polycaprolactone (weight average molecular weight 50000). The filler is melamine cyanurate (mesh number 10000), and the filler proportion is 25%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 12:
base material polycaprolactone (weight average molecular weight 50000). The filler is melamine cyanurate (mesh number 10000), and the proportion of the filler is 35 percent. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 13:
substrate polycaprolactone (weight average molecular weight 50000). And no filler. The cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the mass of the base material. The product with gel content of 40% is obtained.
Material 14:
base material polycaprolactone (weight average molecular weight 50000). Talcum powder (2000 mesh) as filler, 25% filler. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 15:
base material polycaprolactone (weight average molecular weight 50000). Talcum powder (2000 mesh) as filler, 35% filler. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 16:
substrate polycaprolactone (weight average molecular weight 50000). Filler mica powder (2000 mesh), the filler proportion is 25%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 17:
substrate polycaprolactone (weight average molecular weight 50000). Filler silica (2000 mesh) with a filler proportion of 15%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Material 18:
base material polycaprolactone (weight average molecular weight 50000). Filler silica (2000 mesh) with a filler proportion of 35%. The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product with gel content of 40% is obtained.
Second, performance test
1. Flexural Strength test
The low temperature thermoplastic materials prepared above were tested using a universal mechanical testing machine, and the test results are shown in table 1 (results are flexural modulus, in MPa).
Table 1 flexural strength test results
Numbering 1 2 3 4 5 6 7 8 9
Results 751 998 1320 742 1020 1340 784 1103 1480
Numbering 10 11 12 13 14 15 16 17 18
Results 744 984 1314 412 548 607 522 456 559
2. Traction force test and cooling deformation compression force test
The pressure sensor connected with a computer (provided with special software) is arranged below the head of the plaster model, the heated membrane is placed on the face of the plaster model and stretched and shaped downwards, the membrane is fixed on a base which is not connected with the pressure sensor after stretching, and the computer software records the stress condition change condition from the beginning to the complete cooling process of the membrane, and the result is shown in a table 2 (the result unit is N).
TABLE 2 moulding pulling force test results
Figure BDA0002781966570000121
Figure BDA0002781966570000131
As can be seen from Table 1, the melamine cyanurate has an obvious reinforcing effect on the polycaprolactone low-temperature thermoplastic material, and under the same addition amount, the melamine cyanurate reinforcing material is superior to a common reinforcing filling material, so that the reinforcing effect is better, and the deformation resistance is stronger. When the material is applied to radiotherapy location and makes the location diaphragm, because the location diaphragm effect is fixed patient's head or neck chest etc. position, prevent that radiotherapy in-process patient from removing, consequently, the resistant deformability of diaphragm material is better, and then the fixity after moulding on patient's health is better, adds melamine cyanurate and can show the fixed precision that improves the diaphragm.
As can be seen from Table 2, the cooling deformation compression force of the radiotherapy positioning membrane prepared by adding melamine cyanurate is obviously lower than that of the low-temperature radiotherapy positioning membrane prepared by pure polycaprolactone and other common reinforced filling materials. The lower the cooling compression, the more comfortable the user is in the clinic.
The above effects are obtained when melamine cyanurate is replaced with melamine polyphosphate and/or melamine phosphate, and thus, the description thereof is omitted.
Therefore, the fixing device prepared by the material has higher bending modulus and lower cooling deformation compression force compared with a low-temperature radiotherapy positioning membrane prepared by pure polycaprolactone and other common reinforced filling materials. Namely, the low-temperature thermoplastic material prepared by the invention has smaller contractility after forming, better comfort and better fixing strength, thereby being more suitable for hospitals or other radiotherapy units and being matched with three-dimensional conformal radiotherapy instruments for use in tumor operations.
Example 2
Preparation of materials
1. Method for preparing material
The material was prepared according to the following steps:
(1) the base material, the filler and the crosslinking agent are stirred to obtain a uniform mixture.
(2) In a double-screw granulator, the mixture is melted, blended and extruded into granules, and the melting temperature is between 60 and 150 ℃.
(3) And (3) rolling and molding the granules in an extrusion rolling device, wherein the processing temperature is between 60 and 150 ℃.
(4) Irradiating the sheet material by a linear accelerator with gamma ray at an irradiation dose of 4KGy, and controlling the irradiation time to obtain the low-temperature thermoplastic material with the required gel content.
2. Gel content determination method
The gel content was measured in the same manner as in example 1.
Material 19:
substrate polycaprolactone (weight average molecular weight 40000). Melamine cyanurate (a mixture of 2000 mesh and 10000 mesh) with a filler proportion of 25% (10% and 15% for each). The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product was obtained with a gel content of 30%.
Material 20:
substrate polycaprolactone (weight average molecular weight 80000). Melamine cyanurate (a mixture of 2000 mesh and 10000 mesh) with a filler proportion of 25% (10% and 15% for each). The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.2 percent of the total mass of the base material and the filler. The product was obtained with a gel content of 30%.
Second, performance test
The test method was the same as in example 1, and the results are shown in Table 3.
Table 3 example 2 test results
Figure BDA0002781966570000151
Example 3
Preparation of materials
1. Method for preparing material
The material was prepared according to the following steps:
(1) the base material, the filler and the crosslinking agent are stirred to obtain a uniform mixture.
(2) In a double-screw granulator, the mixture is melted, blended and extruded into granules, and the melting temperature is between 60 and 150 ℃.
(3) And (3) rolling and molding the granules in an extrusion rolling device, wherein the processing temperature is between 60 and 150 ℃.
(4) Irradiating the sheet material with gamma rays through a linear accelerator, and controlling the irradiation time to obtain the low-temperature thermoplastic material with the required gel content.
2. Gel content determination method
The gel content was measured in the same manner as in example 1.
Material 21:
base material polycaprolactone (weight average molecular weight 50000). Melamine cyanurate (a blend of 2000 mesh and 10000 mesh) with a filler ratio of 25% (10% and 15% for both ratios). The dosage of the cross-linking agent triallyl isocyanurate accounts for 0.05 percent of the total mass of the base material and the filler. The irradiation dose was 5KGy, and a product having a gel content of 20% was obtained.
Material 22:
base material polycaprolactone (weight average molecular weight 50000). Melamine cyanurate (a mixture of 2000 mesh and 10000 mesh) with a filler proportion of 25% (10% and 15% for each). The cross-linking agent triallyl isocyanurate accounts for 5 percent of the total mass of the base material and the filler. The irradiation dose was 5KGy, and a product having a gel content of 50% was obtained.
Material 23:
base material polycaprolactone (weight average molecular weight 50000). Melamine cyanurate (a mixture of 2000 mesh and 10000 mesh) with a filler proportion of 25% (10% and 15% for each). The cross-linking agent triallyl isocyanurate accounts for 5 percent of the total mass of the base material and the filler. The irradiation dose was 10kGy, and a product with a gel content of 70% was obtained.
Material 24:
base material polycaprolactone (weight average molecular weight 50000). Melamine cyanurate (a blend of 2000 mesh and 10000 mesh) with a filler ratio of 25% (10% and 15% for both ratios). The cross-linking agent triallyl isocyanurate accounts for 5 percent of the total mass of the base material and the filler. The irradiation dose was 30kGy, and a product with 100% gel content was obtained.
Second, performance test
The test method was the same as in example 1, and the results are shown in Table 4.
Table 4 example 3 test results
Figure BDA0002781966570000161
Figure BDA0002781966570000171

Claims (6)

1. A process for preparing a melamine salt reinforced low temperature thermoplastic material comprising the steps of:
(1) mixing polycaprolactone, melamine salt and a cross-linking agent to obtain a composition; wherein the melamine salt is melamine cyanurate, melamine polyphosphate or melamine phosphate, and the mass ratio of polycaprolactone to melamine salt is 90:10-60: 40; the mesh number of the melamine salt is 800-10000 meshes; the cross-linking agent is selected from triallyl isocyanurate, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, pentaerythritol triacrylate and ethylene dimethacrylate, and the dosage of the cross-linking agent is 0.05 to 5 percent of the total mass of polycaprolactone and melamine salt;
(2) carrying out a molding process on the uniformly mixed composition to obtain a blank;
(3) performing a cross-linking process on the blank to obtain a melamine salt reinforced low-temperature thermoplastic material with the gel content of more than or equal to 20%; the specific determination method of the gel content comprises the following steps: weighing a sample with the mass of m1, putting the sample into a ground bottle filled with 25mL of toluene, covering a bottle cap, putting the bottle cap into a constant-temperature oven at 25 ℃ to swell for 48 hours, taking out the sample, extracting the sample for 24 hours, drying the sample in a vacuum oven at 50 ℃ until the mass of the sample is constant, and weighing the sample with the mass of m2, wherein the gel content is Vc = m2/m1 multiplied by 100%.
2. The method of claim 1, wherein the crosslinking process in step (3) is irradiation crosslinking.
3. The method of claim 1, wherein the polycaprolactone of step (1) has a weight average molecular weight of 40000-.
4. A melamine salt reinforced low temperature thermoplastic material, characterized in that it is obtainable by a process according to any one of claims 1 to 3.
5. Use of a melamine salt reinforced low temperature thermoplastic material obtainable by a process according to any one of claims 1 to 3 for the preparation of a device for immobilising a part or joint of the human body.
6. A device for immobilisation of a part or joint of the human body, the body of which is made of a melamine salt reinforced low temperature thermoplastic material prepared according to any one of claims 1 to 3.
CN202011284739.1A 2020-11-17 2020-11-17 Melamine salt reinforced low-temperature thermoplastic material and preparation method thereof Active CN112480616B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202011284739.1A CN112480616B (en) 2020-11-17 2020-11-17 Melamine salt reinforced low-temperature thermoplastic material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202011284739.1A CN112480616B (en) 2020-11-17 2020-11-17 Melamine salt reinforced low-temperature thermoplastic material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN112480616A CN112480616A (en) 2021-03-12
CN112480616B true CN112480616B (en) 2022-08-23

Family

ID=74931638

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202011284739.1A Active CN112480616B (en) 2020-11-17 2020-11-17 Melamine salt reinforced low-temperature thermoplastic material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN112480616B (en)

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4481322A (en) * 1983-03-30 1984-11-06 Union Carbide Corporation Novel reinforcing additive and method of reinforcing thermoplastic polymer therewith
CN101698743B (en) * 2009-09-11 2012-03-28 广州科莱瑞迪医疗器材有限公司 Low-temperature thermoplastic material and preparation method thereof
WO2013045965A1 (en) * 2011-09-28 2013-04-04 Italmatch Chemicals S.P.A. Halogen-free flame retardant polyesters composition
CN104788923A (en) * 2015-04-20 2015-07-22 广州迈得菲明医疗器械有限公司 Novel low-temperature thermoplastic material and preparation method thereof
CN108084676A (en) * 2016-11-22 2018-05-29 广州天泓医疗科技有限公司 A kind of low-temp thermoplastic material
CN110452511A (en) * 2019-08-23 2019-11-15 南京茂宇医疗器械科技有限公司 A kind of low temperature shape memory high molecule material and preparation method thereof

Also Published As

Publication number Publication date
CN112480616A (en) 2021-03-12

Similar Documents

Publication Publication Date Title
CN101698743B (en) Low-temperature thermoplastic material and preparation method thereof
US5540876A (en) Gamma radiation treated material
JP6209529B2 (en) Method for producing a polymer sheet for use as a fastening element
KR20070078078A (en) Surgical implant and manufacturing method
US8859691B2 (en) Low temperature thermoplastic material and preparing method thereof
CN101062977B (en) Low-temperature thermoplastic material and preparation technique thereof
CN1887364A (en) Biodegradable medical extracorporeal fixing material possessing shape memory function
BR112012009194B1 (en) METHOD FOR PRODUCING FIBER-REINFORCED COMPOSITE MATERIAL, AND HEAT RESISTANT MOLDING MATERIAL AND HEAT RESISTANT STRUCTURAL MATERIAL USING THE COMPOSITE MATERIAL
BE1008800A7 (en) Foamed thermoplastic material.
US9827442B2 (en) Thermoplastic sheet, a radiation mask of thermoplastic sheet and method for providing said sheet and said mask
CN112480616B (en) Melamine salt reinforced low-temperature thermoplastic material and preparation method thereof
CN112375352B (en) Low-temperature thermoplastic material and preparation method thereof
CN111698972B (en) Fixing device
CN104788923A (en) Novel low-temperature thermoplastic material and preparation method thereof
CN108478884B (en) Shape memory high-thermal conductivity medical external fixation multilayer material and preparation method thereof
CN1357388A (en) New-type medical bandage
CN110452511A (en) A kind of low temperature shape memory high molecule material and preparation method thereof
CN116804111A (en) Color-changeable low-temperature thermoplastic material and preparation method and application thereof
Jones et al. Application of trans‐1, 4 polyisoprene in orthopedic and rehabilitation medicine
CN113907937A (en) Preparation method of fracture fixator, fracture fixator and use method of fracture fixator
WO2020006615A1 (en) Method for producing a polymer composite for use in orthopaedic devices and products thus produced
CN115850902B (en) Breathing pipe with high temperature sensitivity and rebound resilience, and preparation process and application thereof
KR102574889B1 (en) Bolus forming material and bolus using the same
CN118006099A (en) Low-temperature thermoplastic medical material and preparation method thereof
EP0593549A1 (en) A material and splint for orthopaedical, surgical and veterinary use.

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant